Evidence map›Paper›PMID 36107237›Full record

ArticlePediatric surgery international2022

Differential expression profiling of onco and tumor-suppressor genes from major-signaling pathways in Wilms' tumor.

Dinesh Kumar Sahu, Neetu Singh, Mumani Das, Jiledar Rawat, Devendra Kumar Gupta

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric surgery international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 44% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Dinesh Kumar Sahu *Molecular Biology Unit, Center for Advance Research, King George's Medical University, Lucknow, India. dinesh23biotech@gmail.com.ORCID http://orcid.org/0000-0002-5040-2046
Neetu Singh *Molecular Biology Unit, Center for Advance Research, King George's Medical University, Lucknow, India. neetuaashi@yahoo.co.in.
Mumani DasRegional Medical Research Centre, Bhubaneswar, India.
Jiledar RawatDepartment of Paediatric Surgery, King George's Medical University, Lucknow, India.
Devendra Kumar GuptaDepartment of Paediatric Surgery, Post Graduate Institute of Child Health, Noida, India.
King George's Medical University · INInstitute of Child Health · INRegional Medical Research Centre · IN

Funding

SCIENCE AND ENGINEERING RESEARCH BOARD (SERB), National Post Doctoral Fellowship award, File no. PDF/2016/001782
6 · The paper itself

Abstract

purposeWilms' tumor is the most-frequent malignant-kidney tumor in children under 3-4 years of age and is caused by genetic alterations of oncogenes (OG) and tumor-suppressor genes (TG). Wilms' tumor has been linked to many OG-&-TG. However, only WT1 has a proven role in the development of this embryonic-tumor.

methodsThe study investigates the level of mRNA expression of 16 OGs and 20 TGs involved in key-signaling pathways, including chromatin modification; RAS; APC; Cell Cycle/Apoptosis; Transcriptional Regulation; PI3K; NOTCH-&-HH; PI3K & RAS of 24-fresh Wilms'-tumor cases by capture-and-reporter probe Code-Sets chemistry, as CNVs in these pathway genes have been reported.

resultsUpon extensively investigating, MEN1, MLL2, MLL3, PBRM1, PRDM1, SMARCB1, SETD2, WT1, PTPN11, KRAS, HRAS, NF1, APC, RB1, FUBP1, BCOR, U2AF1, PIK3CA, PTEN, EBXW7, SMO, ALK, CBL, EP300-and-GATA1 were found to be significantly up-regulated in 58.34, 62.5, 79.17, 91.67, 58, 66.66,54, 58.34, 66.67, 75, 62.5, 62.5, 58, 79.17, 79.17, 75, 70.84, 50, 50, 75, 66.66, 62.50, 61.66, 58.34-and-62.50% of cases respectively, whereas BRAF, NF2, CDH1, BCL2, FGFR3, ERBB2, MET, RET, EGFR-and-GATA2 were significantly down regulated in 58, 87.50, 79.16, 54.16, 79.17, 91.66, 66.66, 58.33, 91.66-and-62.50% of cases, respectively. Interestingly, the WT1 gene was five-fold down regulated in 41.66% of cases only.

conclusionHence, extensive profiling of OGs and TGs association of major-signaling pathways in Wilms' tumor cases may aid in disease diagnosis. PBRM1 (up-regulated in 91.67% of cases), ERBB2 and EGFR (down-regulated in 91.66 and 91.66% of cases, respectively) could be marker genes. However, validation of all relevant results in a larger number of samples is required.

Indexed as

Kidney NeoplasmsWilms TumorChildChromatinClass I Phosphatidylinositol 3-KinasesDNA-Binding ProteinsErbB ReceptorsGenes, SuppressorHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins B-rafProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins p21(ras)Receptor Protein-Tyrosine KinasesRNA-Binding ProteinsRNA, MessengerChromatinClass I Phosphatidylinositol 3-KinasesDNA-Binding ProteinsErbB ReceptorsFUBP1 protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins B-rafProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins p21(ras)Receptor Protein-Tyrosine KinasesRNA-Binding ProteinsRNA, MessengerSplicing Factor U2AFCopy number variationsOncogenesTumor suppressor genesWilms’ tumor

Identifiers

PMID36107237
OpenAlexW4295899665

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.